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Figure 1. Air temperature and rainfall during the study between February 2015 and January 2016 in Intra-annual colonization of Chironomidae on leaf litter in a Brazilian Cerrado stream

Figure 1. Air temperature and rainfall during the study between February 2015 and January 2016 in the Boiadeiro stream, Mucugê, BA, Brazilian Cerrado. Data: http://www.snirh.gov.br/hidroweb/ serieshistoricas (Hidroweb 2020).

Figure 5 in Intra-annual colonization of Chironomidae on leaf litter in a Brazilian Cerrado stream

Figure 5. Non-metric multidimensional scaling (NMDS) of Chironomidae assemblages functional feeding group at leaf litter during inter-annual seasons in Boiadeiro stream, Mucugê, BA, Brazilian Cerrado. RD-Rainy-dry (brown). (D) Dry (red), (DR) Dry-rainy (green), (R) Rainy (blue).

Figures 2–3 in Intra-annual colonization of Chironomidae on leaf litter in a Brazilian Cerrado stream

Figures 2–3. Abundance (2) and richness (3) (mean ± SEM) of Chironomidae assemblages associated at leaf litter on 30, 60, and 90 days during inter-annual seasons in Boiadeiro stream, Mucugê, BA, Brazilian Cerrado.

Figure 4 in Intra-annual colonization of Chironomidae on leaf litter in a Brazilian Cerrado stream

Figure 4. Functional feeding group (FFG) proportion of Chironomidae assemblages associated at leaf litter during inter-annual seasons in Boiadeiro stream, Mucugê, BA, Brazilian Cerrado. (Shr) Shredder, (C-F) Collector-filter, (C-G) Collector-Gatherer, (Scr) Scraper, (Pre) Predator.

FIGURE 8 in Towards the diversity of non-biting midges of the tribe Tanytarsini from Eocene Baltic amber (Diptera: Chironomidae)

FIGURE 8. Stempellinella fibra sp. nov., adult male, holotype. Hypopygium and its structures in dorsal aspect, photographed in reflected light (1, 2), in transmitted light (4) and drawn (3, 5); 4-5, median volsella (5 magnified ca. 2 times relative to 4).

FIGURE 5 in Towards the diversity of non-biting midges of the tribe Tanytarsini from Eocene Baltic amber (Diptera: Chironomidae)

FIGURE 5. Tanytarsus crocota sp. nov., adult male, holotype. Hypopygium and its structures in dorsal (1, 2) and ventral aspect (3, 4), photographed in reflected light (1), transmitted light (3) and drawn (2, 4); 3-4, median volsella (4 magnified ca. 3 times relative to 2 and 3).

FIGURE 2 in Towards the diversity of non-biting midges of the tribe Tanytarsini from Eocene Baltic amber (Diptera: Chironomidae)

FIGURE 2. Rheotanytarsus hoffeinsorum sp. nov., adult male, holotype. 1, as syninclusion in amber (at left); 2, habitus.

FIGURE 1 in Towards the diversity of non-biting midges of the tribe Tanytarsini from Eocene Baltic amber (Diptera: Chironomidae)

FIGURE 1. Tanytarsini - inclusions in Baltic amber from the Hoffeins collection (for details see Table 1 and Material examined).

FIGURE 4 in Towards the diversity of non-biting midges of the tribe Tanytarsini from Eocene Baltic amber (Diptera: Chironomidae)

FIGURE 4. Tanytarsus crocota sp. nov., adult male, holotype. 1, inclusion in amber; 2, habitus; 3-4, wing photographed in transmitted (3) and reflected light (4); 5, spur of fore leg tibia.

FIGURE 7 in Towards the diversity of non-biting midges of the tribe Tanytarsini from Eocene Baltic amber (Diptera: Chironomidae)

FIGURE 7. Stempellinella fibra sp. nov., adult male, holotype. 1, inclusion in amber; 2, habitus; 3, antenna (white arrows: borders between well discernible flagellomeres; grey arrow: incomplete fusion); 4, frontal tubercle (black arrow), antennal pedicel and eye.

FIGURE 6 in Towards the diversity of non-biting midges of the tribe Tanytarsini from Eocene Baltic amber (Diptera: Chironomidae)

FIGURE 6. Variations of diagnostic structures in males of Tanytarsus protogregarius (1, 2) and T. serafini (3-6). Hypopygium in dorsolateral aspect (1, 3, 5) and its structures magnified ca. 3-4 times (below): anal point (2, 4) and superior volsella (6).

FIGURE 3 in Towards the diversity of non-biting midges of the tribe Tanytarsini from Eocene Baltic amber (Diptera: Chironomidae)

FIGURE 3. Rheotanytarsus hoffeinsorum sp. nov., adult male, holotype. Hypopygium and its structures in dorsal (1-3) and ventral aspect (4-6), photographed in reflected light (1, 4, 5) and drawn (2, 3, 6); 3, superior volsella; 5-6, median volsella (6 magnified ca. 2 times relative to 5 and ca. 5 times relative to 4).

Figure 4. Smittium aggregatum. a in A NEW ASSOCIATION BETWEEN HARPELLALES, INSECT-GUT INHABITING FUNGI, AND CHIRONOMIDAE IN JAPAN WITH AN UPDATED LIST OF HARPELLALES DOCUMENTED FROM CHIRONOMIDAE Abstract

Figure 4. Smittium aggregatum. a. Thallus in the hindgut. Arrow: Hindgut cuticle (folded when dissected). Arrowheads: spores. Hyphal aggregation at the basal area of the thallus is the feature of this species. b. Detached spore. Arrowhead: Collar. Appendage is not reported in this species. c. Spore production. Arrowhead: The youngest spore. Scales. a: 20 μm. b–c: 5μm. Specimen ID. a: TNS-F-89237. b and c: TNS-F-89234. National Museum of Nature and Science, Tokyo. Host: larvae of Tanytarsini collected at Enzan Takahashi, Yamanashi, 1300m above sea level. a: water-mounted. b and c: Lactophenol-mounted.

Figure 3. Stachylina pedifer. a in A NEW ASSOCIATION BETWEEN HARPELLALES, INSECT-GUT INHABITING FUNGI, AND CHIRONOMIDAE IN JAPAN WITH AN UPDATED LIST OF HARPELLALES DOCUMENTED FROM CHIRONOMIDAE Abstract

Figure 3. Stachylina pedifer. a. Mature thalli in the peritrophic membrane. Arrows: foot-like shaped basal part penetrating the peritrophic membrane. Arrowheads: folding peritrophic membrane. Also, the same symbols mean the same meaning in figs b, c, and d. b. Higher magnification of the basal part of a thallus. c. Young thallus producing spores. Double arrowheads: spore initial. d. Almost mature thallus with eight spores. *: Spores of adjacent thallus. e. Detached spore. Arrowhead: appendage. Scales. a: 20 μm. b–e: 10μm. Specimen ID. a and b: 140224-1. e: 140225-4. Photos c and d are taken from temporary slides. a, c and d: water-mounted. b and e: Lactophenol-mounted.

Figure 2 in A NEW ASSOCIATION BETWEEN HARPELLALES, INSECT-GUT INHABITING FUNGI, AND CHIRONOMIDAE IN JAPAN WITH AN UPDATED LIST OF HARPELLALES DOCUMENTED FROM CHIRONOMIDAE Abstract

Figure 2. The species number in the two major genera of Harpellales described from Chironomidae (N=139 species)

Figure 1 in A NEW ASSOCIATION BETWEEN HARPELLALES, INSECT-GUT INHABITING FUNGI, AND CHIRONOMIDAE IN JAPAN WITH AN UPDATED LIST OF HARPELLALES DOCUMENTED FROM CHIRONOMIDAE Abstract

Figure 1. Total number of species in Harpellales described from Chironomidae and other hosts (N=270 species.)

Figure 2 in BRYOPHAENOCLADIUS ADIGENSIS SP. N., A NEW SPECIES FROM THE ITALIAN ALPS (CHIRONOMIDAE, ORTHOCLADIINAE)

Figure 2. Type-locality of Bryophaenocladius adigensis sp. n.. The Sardagna stream (left), the confluence between Rio Sardagna and the Adige River (right).

Figure 1 in BRYOPHAENOCLADIUS ADIGENSIS SP. N., A NEW SPECIES FROM THE ITALIAN ALPS (CHIRONOMIDAE, ORTHOCLADIINAE)

Figure 1. Male adult of Bryophaenocladius adigensis sp. n. A) coronal triangle; B) clypeus; C) palpomere 3; D) lobes of antepronotum; E) tibial spurs of PIII; F-G) hypopygium in dorsal and ventral view; H) tergite IX and anal point, lateral; I) inferior volsella, right side; J-K) gonostylus at right and acute angle; L) virga. The arrows indicate some distinguishing characters.

Figure 1 in Chironomidae Collected At The Seashore In Kume Island, Japan

Figure 1. Map of Shinri Beach with the locations of the sampling site (●). This map is based on public survey maps published by the Geospatial Information Authority of Japan.

Figure 6 in SEASONAL VARIATION IN THE CHIRONOMIDAE (DIPTERA) COMMUNITIES OF TWO FAROESE STREAMS Abstract

Figure 6. Non-metric multidimensional scaling (NMDS) plots illustrating the distribution of (a) communities and (b) Chironomidae taxa in the larger stream Sundsá (green) and smaller stream Matará (blue). Significant associations (p <0.05) of the environmental variables to the axes are shown with arrows. Taxa acronyms are listed in Table 2.